ZMP
gli3
Ensembl ID:
ZFIN ID:
Description:
zinc finger protein GLI3 [Source:RefSeq peptide;Acc:NP_991291]
Human Orthologue:
GLI3
Human Description:
GLI family zinc finger 3 [Source:HGNC Symbol;Acc:4319]
Mouse Orthologue:
Gli3
Mouse Description:
GLI-Kruppel family member GLI3 Gene [Source:MGI Symbol;Acc:MGI:95729]
Alleles
There are 8 alleles of this gene:
Allele Name | Consequence | Status | Availability |
---|---|---|---|
sa32478 | Nonsense | Available for shipment | Available now |
hu2965 | Nonsense | Confirmed mutation in F2 line | Not yet available |
sa8416 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa8870 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37838 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa25210 | Nonsense | Mutation detected in F1 DNA | Not yet available |
sa37837 | Nonsense | Mutation detected in F1 DNA | Not yet available |
Mutation Details
Allele Name:
sa32478
Status:
Available for shipment
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058992 | Nonsense | 560 | 1553 | 12 | 15 |
ENSDART00000123554 | Nonsense | 560 | 1553 | 11 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 11316447)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 11403850 |
GRCz11 | 24 | 11544217 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
AACTAATCTTGTTCATTTTTGTCCTTTTTTATCTCAGTTTGAAGGCTGTT[C/A]AAAGGCATATTCCAGATTAGAGAACCTGAAAACACATTTGCGTTCACACA
Long Flanking Sequence:
TTAGTATTTTTACTTAAATTTACTGATTGTTAATAAAGGAATGTGGTATTCTTTGAACTTTGCATAGTTGTAAAAAATAATAATGCTTTTCTCAAAGCATACCACAGCATGACAAAAGTTCCATATCATATTTTTTTATTCATTAACATGACTTTTGACCGACTGTATTCTTCCTCTCACAGCACATAAATAATGACCATATTCATGGAGAAAAAAAGGAATTTGTGTGTCGCTGGGAGGAATGTTCAAGAGAACAGAAACCCTTTAAGGCCCAGTATATGCTGGTGGTGCACATGCGCAGACACACAGGAGAGAAGCCTCATAAATGCACGGTGAGGATTGCATTTAACACATTTGGTACTTGAAGATTTGTGACACTCATTTCAGTAAGGAGAGCTTGCGATCTGGATTTTGGTTTAGTCCAAGAAGCTGCTGTAAAAACCTGTCTATAACTAATCTTGTTCATTTTTGTCCTTTTTTATCTCAGTTTGAAGGCTGTT[C/A]AAAGGCATATTCCAGATTAGAGAACCTGAAAACACATTTGCGTTCACACACAGGAGAGAAGCCATATGTGTGTGAACATGAAGGCTGCAACAAAGCCTTTTCGAATGCATCAGACCGAGCCAAACACCAGAATCGGACACACTCTAATGAGGTCAGTTCACACATGAACCAAGAATGGCATTTTTTAGTTTTTTATTATTATTTTTTTGTTCTAAATATCTCTGCTTTAGACAAGTAGAAAAAATATAAAGAATTTGAAATTAAAATGAAAAGAATTTATGCATTTCTCGTTGCAAATGATAAATAATACATGTCCAAAGCAAAAAAAGCTTAATCCATCTCTGAATTGTCCTTTTTTCAGACATTGCCACATTGTAAAATTTTTCCTGTCATGTTTTGTTGATATCATGCCAGCATTTTAAACATGCAGAAAATTAGTGATGGTTAATTAATTAATTAATGGCTAAAATGGCTAAAATTACTTAACATCTCAAGCTAAA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
hu2965
Status:
Confirmed mutation in F2 line
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058992 | Nonsense | 655 | 1553 | 13 | 15 |
ENSDART00000123554 | Nonsense | 655 | 1553 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 11311698)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 11399101 |
GRCz11 | 24 | 11539468 |
KASP Assay ID:
554-0076.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ATGGTCCTGAAGCCCATGTCACCAAAAAACAACGTGGGGAGACATACCCA[C/T]GACCCCCACCTCAGCCACGAGAACCTGGAGCAACCACTGACCAAAAGGAG
Long Flanking Sequence:
ATGAGAATTACTTGGCACGTAGATGCAATGTGACTTAAATTCAACAAACATACCATCAAAATAAAGTGAGATCGTGAAAATGCATTGCATTAAATATTCTAAAGACATTGGGGTTTATTTTTGTTGTTGTTGTTTTGGAAAGTTATGTTACATATTTATCTTGCAAGCATTGTCAACAATGAAAAAATGTGTAAGTTGACATGGCATGTGTTTTGCATCAGGTGTGAGACTGCTTTTATCGGTTCACTCTTTGAATTTTTGCTGAACTTTTATATAACAGCTACATTGCACTCCACAGAAATGTATAGAATGCATTAGCAAACATTTATTTCTATTATATGCAAATGCTCTTTTTTTATTTCTCTCAGAAACCCTATGTGTGTAAAATTCCTGGCTGCACTAAGCGGTACACTGACCCAAGCTCCTTAAGGAAACATGTTAAAACTGTACATGGTCCTGAAGCCCATGTCACCAAAAAACAACGTGGGGAGACATACCCA[C/T]GACCCCCACCTCAGCCACGAGAACCTGGAGCAACCACTGACCAAAAGGAGTATACCCATGCTACCTCAAAACAGGATGAATGTCTGCAAGTCAAGTCAATCAAAACAGAAAAGCCCATGGTAAGCCTCCTTTCATATCAAAAATCAAAAATAAATAACATTTTATATTTAAAGTATTTAAATTGAAAATTATTAGCTCTACTTTTTTATTTTTTCAAGTATTTCCCAAATGATATTTAACAGAGCAAGGACAGTTCCAGAATTTCATTTTTTTTTTTCTTCTGGAGAAATTTGTTTTATTTTGCCTAGAAAAAAAAAAACAGATTTAGTTTTTAAATACCGTTGTAAGTTCAATGTTATTAACCCCTTTAAGAATTTTTTCCAGATTGTCTTAAAAAAAACAATGACTTGCCTAATTACCCTAACTTGACTAGTTAACTAAAAAAACAAATCTTTTTTTAAAAATCTAGTAAAATATTATGTACTTTCATCAAGGCAAAG
Associated Phenotype:
Normal
Stage | Entity | Quality | Tag |
---|---|---|---|
Larval:Day 5 ZFS:0000037 |
whole organism ZFA:0001094 |
quality PATO:0000001 |
normal PATO:0000461 |
Mutation Details
Allele Name:
sa8416
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058992 | Nonsense | 677 | 1553 | 13 | 15 |
ENSDART00000123554 | Nonsense | 677 | 1553 | 12 | 14 |
ENSDART00000058992 | Nonsense | 677 | 1553 | 13 | 15 |
ENSDART00000123554 | Nonsense | 677 | 1553 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 11311631)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 11399034 |
GRCz11 | 24 | 11539401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGAGAAMCTGGAGCAACCACTGAYCAAAAGGAGTATACCCATGCTACCT[C/A]AAAACAGGATGAATGTCTGCAAGTCAAKTCAATCAAAACAGAAAAGCCCA
Long Flanking Sequence:
GAGATCGTGAAAATGCATTGCATTAAATATTCTAAAGACATTGGGGTTTATTTTTGTTGTTGTTGTTTTGGAAAGTTATGTTACATATTTATCTTGCAAGCATTGTCAACAATGAAAAAATGTGTAAGTTGACATGGCATGTGTTTTGCATCAGGTGTGAGACTGCTTTTATCGGTTCACTCTTTGAATTTTTGCTGAACTTTTATATAACAGCTACATTGCACTCCACAGAAATGTATAGAATGCATTAGCAAACATTTATTTCTATTATATGCAAATGCTCTTTTTTTATTTCTCTCAGAAACCCTATGTGTGTAAAATTCCTGGCTGCACTAAGCGGTACACTGACCCAAGCTCCTTAAGGAAACATGTTAAAACTGTACATGGTCCTGAAGCCCATGTCACCAAAAAACAACGTGGGGAGACATACCCACGACCCCCACCTCAGCCACGAGAACCTGGAGCAACCACTGACCAAAAGGAGTATACCCATGCTACCT[C/A]AAAACAGGATGAATGTCTGCAAGTCAAGTCAATCAAAACAGAAAAGCCCATGGTAAGCCTCCTTTCATATCAAAAATCAAAAATAAATAACATTTTATATTTAAAGTATTTAAATTGAAAATTATTAGCTCTACTTTTTTATTTTTTCAAGTATTTCCCAAATGATATTTAACAGAGCAAGGACAGTTCCAGAATTTCATTTTTTTTTTTCTTCTGGAGAAATTTGTTTTATTTTGCCTAGAAAAAAAAAAACAGATTTAGTTTTTAAATACCGTTGTAAGTTCAATGTTATTAACCCCTTTAAGAATTTTTTCCAGATTGTCTTAAAAAAAACAATGACTTGCCTAATTACCCTAACTTGACTAGTTAACTAAAAAAACAAATCTTTTTTTAAAAATCTAGTAAAATATTATGTACTTTCATCAAGGCAAAGATAAAACAAATCAGTTATTAGAAATTAATCTTCAAAACTAATATATTTAAAAATGTGTTGGAAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa8870
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058992 | Nonsense | 677 | 1553 | 13 | 15 |
ENSDART00000123554 | Nonsense | 677 | 1553 | 12 | 14 |
ENSDART00000058992 | Nonsense | 677 | 1553 | 13 | 15 |
ENSDART00000123554 | Nonsense | 677 | 1553 | 12 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 11311631)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 11399034 |
GRCz11 | 24 | 11539401 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
ACGAGAAMCTGGAGCAACCACTGAYCAAAAGGAGTATACCCATGCTACCT[C/A]AAAACAGGATGAATGTCTGCAAGTCAAKTCAATCAAAACAGAAAAGCCCA
Long Flanking Sequence:
GAGATCGTGAAAATGCATTGCATTAAATATTCTAAAGACATTGGGGTTTATTTTTGTTGTTGTTGTTTTGGAAAGTTATGTTACATATTTATCTTGCAAGCATTGTCAACAATGAAAAAATGTGTAAGTTGACATGGCATGTGTTTTGCATCAGGTGTGAGACTGCTTTTATCGGTTCACTCTTTGAATTTTTGCTGAACTTTTATATAACAGCTACATTGCACTCCACAGAAATGTATAGAATGCATTAGCAAACATTTATTTCTATTATATGCAAATGCTCTTTTTTTATTTCTCTCAGAAACCCTATGTGTGTAAAATTCCTGGCTGCACTAAGCGGTACACTGACCCAAGCTCCTTAAGGAAACATGTTAAAACTGTACATGGTCCTGAAGCCCATGTCACCAAAAAACAACGTGGGGAGACATACCCACGACCCCCACCTCAGCCACGAGAACCTGGAGCAACCACTGACCAAAAGGAGTATACCCATGCTACCT[C/A]AAAACAGGATGAATGTCTGCAAGTCAAGTCAATCAAAACAGAAAAGCCCATGGTAAGCCTCCTTTCATATCAAAAATCAAAAATAAATAACATTTTATATTTAAAGTATTTAAATTGAAAATTATTAGCTCTACTTTTTTATTTTTTCAAGTATTTCCCAAATGATATTTAACAGAGCAAGGACAGTTCCAGAATTTCATTTTTTTTTTTCTTCTGGAGAAATTTGTTTTATTTTGCCTAGAAAAAAAAAAACAGATTTAGTTTTTAAATACCGTTGTAAGTTCAATGTTATTAACCCCTTTAAGAATTTTTTCCAGATTGTCTTAAAAAAAACAATGACTTGCCTAATTACCCTAACTTGACTAGTTAACTAAAAAAACAAATCTTTTTTTAAAAATCTAGTAAAATATTATGTACTTTCATCAAGGCAAAGATAAAACAAATCAGTTATTAGAAATTAATCTTCAAAACTAATATATTTAAAAATGTGTTGGAAAGTA
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37838
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
T > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058992 | Nonsense | 855 | 1553 | 15 | 15 |
ENSDART00000123554 | Nonsense | 855 | 1553 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 11304239)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 11391642 |
GRCz11 | 24 | 11532009 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
GGTGCCTCCATGCCCTGAGCCGTCCAACACAGAGCTGACAATTCTGAGTT[T/A]GCTGCATGAACGACGGGACAGTAGTGGCAGCAACACTAGCTCAGCTTACC
Long Flanking Sequence:
CCTCCAACACCGCCCCCTAAAGGCCAGGCCATGCCTGCCCTCACAGGAAAGGGTAAGTCTTATTTTCTGAGCTCTGTCAACATATCAGACTTTACTAATTGAATTGCAGACCCACAAGCATTTTTATAATCTTTTAAACGTGTTATCCAAAAAAATAAAAAACTGTCATCATCTTCATCTCATTTCAAACCTGTATTTTTATTTTAAAGAAGTGACATTGAAGTAATTTTCACAATGTTACATCTGTTCTTTCAGTAATGCACAGTTTAAAGACATGATGACAGAAGTTTATTTTTAGAGTGTCTGTGGGGTTGTAAAAGGTAGTAAATGAAGTTAGCCAAAATTAAGGACATTAAAAAGTATTAAAAAGTAACAAACATCATCTGACGAGGTATTACATTTTACATCTGTATTATCAGGTCAATGCCTTGGGAGGAGTACTTCTGTGAGGGTGCCTCCATGCCCTGAGCCGTCCAACACAGAGCTGACAATTCTGAGTT[T/A]GCTGCATGAACGACGGGACAGTAGTGGCAGCAACACTAGCTCAGCTTACCTGAGCAGCAGCCGTCGCTCATCTGGCATCTCCCCCTGCTTTTCCAGTCGCTGTTCTAGCCAGGCTTCACTGTCAGAGTACAGCCCCCATCGACATATCCATAATCTCAGTGCAACTGATTCTTATGACCCTATTTCCACTGATGCCTCTCGACGCTCCAGTGAAGCCAGCCAGTATGATGGAGGAAGTTCAAGTGCAGTGGTGTTTGGTGGAAGTGGAGTTTTCAAGGGCAGTGGTATGGGATCAAGAGGGGATCTGAACCTCACTCCAGCTCAACACTATAGCCTAAAGGCCAAGTATGCAGCAGCAACAGGTGGACCGCCTCCCACACCCTTGCCCAGTATGGGGCATATAAACCTAAAGAGTCACTTTGCTTTAAAGGAAGACAGAAAGGACACTGGCCAGCTTACACTACCACCACTGGTCAGGTCACGTCGCTGTAGTGATGGTG
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa25210
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > A
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058992 | Nonsense | 1080 | 1553 | 15 | 15 |
ENSDART00000123554 | Nonsense | 1080 | 1553 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 11303564)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 11390967 |
GRCz11 | 24 | 11531334 |
KASP Assay ID:
554-7352.1 (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
TGGCTTGCCACAAGTACGACATTTCAGTAGTTTAAACAATATGACTTCAT[C/A]ACCCAATCCTGCTAGTTATGGTTACTTAAACAGAGAAGATCACAGTCTGA
Long Flanking Sequence:
TGACCCTATTTCCACTGATGCCTCTCGACGCTCCAGTGAAGCCAGCCAGTATGATGGAGGAAGTTCAAGTGCAGTGGTGTTTGGTGGAAGTGGAGTTTTCAAGGGCAGTGGTATGGGATCAAGAGGGGATCTGAACCTCACTCCAGCTCAACACTATAGCCTAAAGGCCAAGTATGCAGCAGCAACAGGTGGACCGCCTCCCACACCCTTGCCCAGTATGGGGCATATAAACCTAAAGAGTCACTTTGCTTTAAAGGAAGACAGAAAGGACACTGGCCAGCTTACACTACCACCACTGGTCAGGTCACGTCGCTGTAGTGATGGTGCACACAACTCGCATGACAGTCAAGCCGTGTATCAACGAAAGGGAACATACTTTGGTGGTGGTCCAGGGAAAAATGATCGAAGAGCTAGTGATCCTACACATCACAAACAAAATCTTAGTTCTTATGGCTTGCCACAAGTACGACATTTCAGTAGTTTAAACAATATGACTTCAT[C/A]ACCCAATCCTGCTAGTTATGGTTACTTAAACAGAGAAGATCACAGTCTGAACCTACAGAATTCCACCTGTCACGTAGATAGCTTTCAGAGTGGTCTGCACTCCCCTTGTCCTCCTAGCATCATGGAGCAATCAGCACTTGAGAACATTTCCATAAACCAGGATGGTCTTTTGTTACGTGTCAATGAAAACATCCAGTCTGACTTCATGCAGTATCTCCATTCCCAAGATCAGGAATCAATAATTAACCAAGACAACCATAGGCCTATTTTCAATCCCGCAAATGACCAGAACTTCCTCAGTCCACAGCAGCACCAAGAGGGAGTAGAGCAAGAAGACACTAGTATTGATCTGATGCCTATCCAGTCGAATGAAGTGAGCTCTGGTAGTGCCGATGTTACCATTCCAAGGCAGCCGTTTCAGAGGTGTGGCAGATGGTCAGACCAGAGTGGCTCAGTAAGCAACGCCTTTGGTCGATTTGGAAACATGGTTGTACAACAGC
Associated Phenotype:
Not determined
Mutation Details
Allele Name:
sa37837
Status:
Mutation detected in F1 DNA
For more information about the meaning of this status and other statuses, please see our FAQs.
For more information about the meaning of this status and other statuses, please see our FAQs.
Availability:
Not yet available
Mutation:
C > T
Consequence:
Nonsense
Transcripts:
Transcript ID | Consequence | Amino Acid Affected | Amino Acid Total | Exon Affected | Exon Total |
---|---|---|---|---|---|
ENSDART00000058992 | Nonsense | 1390 | 1553 | 15 | 15 |
ENSDART00000123554 | Nonsense | 1390 | 1553 | 14 | 14 |
Genomic Location (Zv9):
Chromosome 24 (position 11302635)
Other Location(s):
Assembly | Chromosome | Position |
---|---|---|
GRCz10 | 24 | 11390038 |
GRCz11 | 24 | 11530405 |
KASP Assay ID:
None (used for ordering genotyping assays)
KASP Sequence:
None
Flanking Sequence:
ACTCCACTAGGCAGGATATTAACAGCCATAATGTACAATCATGCCATCCA[C/T]AAAGCTTGAACAATAGACTAGGCACAAATTGTTCCCCTTCAAATCAGGTT
Long Flanking Sequence:
GCAGATGGTCAGACCAGAGTGGCTCAGTAAGCAACGCCTTTGGTCGATTTGGAAACATGGTTGTACAACAGCAGCCTATAGATTTTATTGATCAGCACTCAGCTCTTCAACACATGGGAGGTATAAGCTATGGGTGCAGAAATTCAGAGCAGCATCTACAAGTAGCAAAACCAGCCCAAGAGAAGTCCAGGATGAAAACAGGCATTAAGACTGAGTCTTCCTCAACCTTCCAACTGGAATCCAAACACAGCAACTTTGGTCGACCAGACTTCTCTCATATCTTTTCGGCCCCCATTCATCAAAAATGTTCCCAGCATACAGTTGTATCCCAATCTTATCCCCAACAAAATCAAATTACAAATCAAGATAGCAGCAACCTCTTTTTGCAAAGACCAGGTAACTGCAGCTTACTCTTGGCTTACCGGCCTCAGCCAGCTGTCAACACTTCCTACTCCACTAGGCAGGATATTAACAGCCATAATGTACAATCATGCCATCCA[C/T]AAAGCTTGAACAATAGACTAGGCACAAATTGTTCCCCTTCAAATCAGGTTTCCGTTGTGAAGCTTGATCAAGTTAATCACCTTCAAATCAACTCTTGCTCATCAATTCAGCAACAAACACCTGTGTTTATTGATAAGTGTTTTGACCTAGAAAAGTCCAAGCTCTCTCACGCCATAGTACAGTCATGTCTAATGGAATCATTGATGGCAGAGAAAGAAAGAACTTCCAAAGTTCTTCTGTCATCTGGGGTTGGTCAGGTGACTAGCACAGTAGAAAGAAGCCCAGCTGAAAAAGTTGGTTTAGGAATTTGTTCCATTGGTGATGATAGTTATGATCAGGGCAGTGTAGTGTCTTCCTCTCAACTCAGTAATTCTCATGATTCCTTTGCATTTCACAGTGTGAATCCAGGCACTAACAACATGGCTATTAGTGACATGAGCTCCCTCCTCACCACCCTCGCAGAAGAGAGTAAATTTCTGGCAATCATCCAATAGTTTGTG
Associated Phenotype:
Not determined